| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 901 | ||
Name | CCNG2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.200C>T; p.A67V; 4:77159428-77159428 |
breast | carcinoma | Substitution - Missense |
c.712G>T; p.D238Y; 4:77164280-77164280 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.712G>T; p.D238Y; 4:77164280-77164280 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.633C>G; p.L211L; 4:77161675-77161675 |
breast | carcinoma | Substitution - coding silent |
c.301_302insT; p.G102fs*10; 4:77160745-77160746 |
liver | carcinoma | Insertion - Frameshift |
c.723C>A; p.F241L; 4:77164291-77164291 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.723C>A; p.F241L; 4:77164291-77164291 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1002C>T; p.F334F; 4:77165891-77165891 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.547G>T; p.D183Y; 4:77161499-77161499 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.488A>T; p.H163L; 4:77160932-77160932 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1035G>T; p.*345Y; 4:77165924-77165924 |
large_intestine; colon | carcinoma; adenocarcinoma | Nonstop extension |
c.790G>C; p.D264H; 4:77164358-77164358 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.366T>C; p.T122T; 4:77160810-77160810 |
skin | malignant_melanoma | Substitution - coding silent |
c.300C>T; p.C100C; 4:77160744-77160744 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.394A>T; p.K132*; 4:77160838-77160838 |
central_nervous_system; brain | glioma | Substitution - Nonsense |
c.791A>G; p.D264G; 4:77164359-77164359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.502A>G; p.I168V; 4:77160946-77160946 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.673G>A; p.E225K; 4:77161715-77161715 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1002delC; p.F334fs*>11; 4:77165891-77165891 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Deletion - Frameshift |
c.591C>T; p.I197I; 4:77161543-77161543 |
skin | malignant_melanoma | Substitution - coding silent |
c.470C>T; p.T157I; 4:77160914-77160914 |
skin | malignant_melanoma | Substitution - Missense |
c.1018C>T; p.L340L; 4:77165907-77165907 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.943G>A; p.E315K; 4:77165832-77165832 |
breast | carcinoma | Substitution - Missense |
c.349T>C; p.C117R; 4:77160793-77160793 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.583C>T; p.R195*; 4:77161535-77161535 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Nonsense |
c.21G>A; p.E7E; 4:77158553-77158553 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1002C>A; p.F334L; 4:77165891-77165891 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.21G>A; p.E7E; 4:77158553-77158553 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.380G>A; p.R127Q; 4:77160824-77160824 |
oesophagus | carcinoma | Substitution - Missense |
c.948G>A; p.E316E; 4:77165837-77165837 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.262T>C; p.L88L; 4:77159490-77159490 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.281A>G; p.K94R; 4:77160725-77160725 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.71A>G; p.Y24C; 4:77158603-77158603 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.938G>A; p.C313Y; 4:77165827-77165827 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.823C>T; p.R275C; 4:77164391-77164391 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.732G>C; p.W244C; 4:77164300-77164300 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.198A>G; p.L66L; 4:77159426-77159426 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.340_342delGAA; p.E114delE; 4:77160784-77160786 |
breast | carcinoma | Deletion - In frame |
c.340_342delGAA; p.E114delE; 4:77160784-77160786 |
large_intestine | carcinoma; adenocarcinoma | Deletion - In frame |
c.205delT; p.F70fs*22; 4:77159433-77159433 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.721_723delTTC; p.F242delF; 4:77164289-77164291 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - In frame |
c.962C>T; p.S321F; 4:77165851-77165851 |
skin | malignant_melanoma | Substitution - Missense |
c.792T>C; p.D264D; 4:77164360-77164360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.792T>C; p.D264D; 4:77164360-77164360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.10T>G; p.L4V; 4:77158542-77158542 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.760G>A; p.E254K; 4:77164328-77164328 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.312T>C; p.C104C; 4:77160756-77160756 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.522A>T; p.S174S; 4:77160966-77160966 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |